Discovery of Novel Pimprinine and Streptochlorin Derivatives as Potential Antifungal Agents

Pimprinine and streptochlorin are indole alkaloids derived from marine or soil microorganisms. In our previous study, they were promising lead compounds due to their potent bioactivity in preventing many phytopathogens, but further structural modifications are required to improve their antifungal activity. In this study, pimprinine and streptochlorin were used as parent structures with the combination strategy of their structural features. Three series of target compounds were designed and synthesized. Subsequent evaluation for antifungal activity against six common phytopathogenic fungi showed that some of thee compounds possessed excellent effects, and this is highlighted by compounds 4a and 5a, displaying 99.9% growth inhibition against Gibberella zeae and Alternaria Leaf Spot under 50 mu g/mL, respectively. EC50 values indicated that compounds 4a, 5a, 8c, and 8d were even more active than Azoxystrobin and Boscalid. SAR analysis revealed the relationship between 5-(3 '-indolyl)oxazole scaffold and antifungal activity, which provides useful insight into the development of new target molecules. Molecular docking models indicate that compound 4a binds with leucyl-tRNA synthetase in a similar mode as AN2690, offering a perspective on the mode of action for the study of its antifungal activity. These results suggest that compounds 4a and 5a could be regarded as novel and promising antifungal agents against phytopathogens due to their valuable potency.

Automated summary

In this study, a series of compounds were designed and synthesized based on the combination strategy of pimprinine and streptochlorin. The evaluation of their antifungal activity showed that compounds 4a and 5a displayed excellent effects against two common phytopathogenic fungi. SAR analysis revealed the relationship between the 5-(3'-indolyl)oxazole scaffold and antifungal activity. Molecular docking models provided insight into the mode of action for compound 4a. These results highlight the potential of compounds 4a and 5a as novel antifungal agents.